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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382793Generated: November 2, 2026

m-Anisoyl chloride → HCID 136063643, compound

https://huagongshe.com/reaction/2382793

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Anisoyl chlorideHCID 74374—
ReactantHCID 25216183HCID 25216183—
ProductHCID 136063643HCID 13606364341%

Reaction Steps

The title compound was prepared following procedure described for intermediate B1, but starting from tert-butyl 2-(2-amino[1,2,4]triazolo[1,5-a]pyridin-5-yl)-1H-pyrrole-1-carboxylate ((A6), 50 mg; 0.17 mmol; 1.0 eq.) and m-anisoyl chloride (57 mg; 0.33 mmol; 2.0 eq.). Further treatment with a DCM/TFA solution (2:1) and purification by flash chromatography on silica (EtOAc/c-Hex, gradient from 50:60 to 80:20) gave the title compound as a white solid (23.1 mg, 41%). HPLC, Rt: 3.40 min. (purity 94.7%). LC/MS, M+(ESI): 334.3, M+(ESI): 332.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-13b81516fa3a4b759aa15ee930bceb3b
Source noteuspto-grants-2012_09